From arterial hypertension complications to von Hippel-Lindau syndrome diagnosis

Von Hippel-Lindau syndrome is a rare, genetically based, autosomal dominant disorder. Its course is accompanied by the development of multiple neoplasms with the following tumours diagnosed most commonly in the central nervous system haemangioblastoma, clear cell renal cell carcinoma, phaeochromocyt...

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Detalles Bibliográficos
Autores principales: Kozaczuk, Sylwia, Ben-Skowronek, Iwona
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2015
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4535675/
https://www.ncbi.nlm.nih.gov/pubmed/26268347
http://dx.doi.org/10.1186/s13052-015-0158-y

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4535675/
https://www.ncbi.nlm.nih.gov/pubmed/26268347
http://dx.doi.org/10.1186/s13052-015-0158-y

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